Search Results - "Medical genetics

miRDM-rfGA: Genetic algorithm-based identification of a miRNA set for detecting type 2 diabetes by Aron Park, Seungyoon Nam

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Genetic analysis of parathyroid and pancreatic tumors in a patient with multiple endocrine neoplasia type 1 using whole-exome sequencing by Bo-Young Kim, Mi-Hyun Park, Hae-Mi Woo, Hye-Yeong Jo, Ji Hoon Kim, Hyung Jin Choi, Soo Kyung Koo

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Genetic analysis of the GLUT10 glucose transporter (<it>SLC2A10</it>) polymorphisms in Caucasian American type 2 diabetes by Mychaleckyj Josyf C, Bowden Donald W, Bento Jennifer L, Hirakawa Shohei, Rich Stephen S, Freedman Barry I, Segade Fernando

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The role of <it>IREB2 </it>and transforming growth factor beta-1 genetic variants in COPD: a replication case-control study by Stolk Jan, MacNee William, Keatings Vera, Donnelly Seamas C, Millar Ann B, Morgan Kevin, Rabinovich Roberto, Roca Josep, Guetta-Baranes Tamar, Alsaegh Aiman, Lotya Juzer, Daly Leslie, Chappell Sally L, Hiemstra Pieter S, Miniati Massimo, Monti Simonetta, O'Connor Clare M, Kalsheker Noor

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Generation of Genetically Stable Human Direct-Conversion-Derived Neural Stem Cells Using Quantity Control of Proto-oncogene Expression by Kwon Daekee, Han Mi-Jung, Ji Minjun, Ahn Hee-Jin, Seo Kwang-Won, Kang Kyung-Sun

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Phylogeography and Genetic Diversity of Human Hydatidosis in Bordering the Caspian Sea, Northern Iran by Focusing on Echinococcus granulosus Sensu Stricto Complex by Abolghasem SIYADATPANAH, Ahmad DARYANI, Shahabeddin SARVI, Adel SPOTIN, Mehdi SHARIF, Reza ESMAEELZADEH DIZAJI, Davood ANVARI, Amir EMAMI ZEYDI, Mohammad Hasan KOHANSAL, Nelson Ivan AGUDELO HIGUITA, Seyed Abdollah HOSSEINI, Mojgan ARYAEIPOUR, Shirzad GHOLAMI

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Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups by Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier

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Environmental and Genetic Determinants of Major Chronic Disease in Beijing-Tianjin-Hebei Region: Protocol for a Community-Based Cohort Study by Kuo Liu, Kuo Liu, Han Cao, Han Cao, Chunyue Guo, Chunyue Guo, Li Pan, Li Pan, Ze Cui, Jixin Sun, Wei Zhao, Xiaoyan Han, Han Zhang, Zhengfang Wang, Kaijun Niu, Naijun Tang, Guangliang Shan, Guangliang Shan, Ling Zhang, Ling Zhang

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Genetic polymorphisms located in genes related to immune and inflammatory processes are associated with end-stage renal disease: a preliminary study by Jimenez-Sousa Ma, López Elisabeth, Fernandez-Rodríguez Amanda, Tamayo Eduardo, Fernández-Navarro Pablo, Segura-Roda Laura, Heredia María, Gómez-Herreras José I, Bustamante Jesús, García-Gómez Juan, Bermejo-Martin Jesús F, Resino Salvador

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A consideration of CYP2D6 genetic variations in the Ghanaian population as a potential 'culprit' for the tramadol 'abuse crisis' by Nicholas Ekow Thomford, Susanna Aba Abraham, Samuel Badu Nyarko, Robert Peter Biney

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Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction by Reza Jabbari, Javad Jabbari, Charlotte Glinge, Bjarke Risgaard, Stefan Sattler, Bo Gregers Winkel, Christian Juhl Terkelsen, Hans-Henrik Tilsted, Lisette Okkels Jensen, Mikkel Hougaard, Stig Haunsø, Thomas Engstrøm, Christine M. Albert, Jacob Tfelt-Hansen

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The association between genetic polymorphisms in ABCG2 and SLC2A9 and urate: an updated systematic review and meta-analysis by Thitiya Lukkunaprasit, Sasivimol Rattanasiri, Saowalak Turongkaravee, Naravut Suvannang, Atiporn Ingsathit, John Attia, Ammarin Thakkinstian

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Establishment of the early prediction models of low-birth-weight reveals influential genetic and environmental factors: a prospective cohort study by Satoshi Mizuno, Satoshi Nagaie, Gen Tamiya, Shinichi Kuriyama, Taku Obara, Mami Ishikuro, Hiroshi Tanaka, Kengo Kinoshita, Junichi Sugawara, Masayuki Yamamoto, Nobuo Yaegashi, Soichi Ogishima

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Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype by Brioschi Simona, Gualandi Francesca, Scotton Chiara, Armaroli Annarita, Bovolenta Matteo, Falzarano Maria S, Sabatelli Patrizia, Selvatici Rita, D'Amico Adele, Pane Marika, Ricci Giulia, Siciliano Gabriele, Tedeschi Silvana, Pini Antonella, Vercelli Liliana, De Grandis Domenico, Mercuri Eugenio, Bertini Enrico, Merlini Luciano, Mongini Tiziana, Ferlini Alessandra

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Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective study by Nan Guo, Huili Xue, Bin Liang, Hailong Huang, Meiying Cai, Liangpu Xu

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DNA-testing for <it>BRCA1/2</it> prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-direct by Sie Aisha S, Spruijt Liesbeth, van Zelst-Stams Wendy AG, Mensenkamp Arjen R, Ligtenberg Marjolijn J, Brunner Han G, Prins Judith B, Hoogerbrugge Nicoline

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The association between genetic variants in <it>hMLH1 </it>and <it>hMSH2 </it>and the development of sporadic colorectal cancer in the Danish population by Syvänen Ann-Christine, Olsen Anja, Tjønneland Anne, Koed Karen, Wiuf Carsten, Wikman Friedrik P, Madsen Bo E, Christensen Lise, Andersen Claus L, Ørntoft Torben F

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Genetic Evidence for the Causal Link Between Coagulation Factors and the Risk of Ovarian Cancer: A Two-Sample Mendelian Randomization Study by Dai T, Jia Y, Zhang Y

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Combined Effect of CYP2C19 Genetic Polymorphisms and C-Reactive Protein on Voriconazole Exposure and Dosing in Immunocompromised Children by Juan Chen, Ying Wu, Yuelin He, Xiaoqin Feng, Yuqiong Ren, Shiting Liu

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Identifying significant genetic regulatory networks in the prostate cancer from microarray data based on transcription factor analysis and conditional independency by Yeh Cheng-Yu, Lin Yu-Chun, Cheng Shih-Wu, Yeh Hsiang-Yuan, Lin Shih-Fang, Soo Von-Wun

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